학술논문

AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale
Document Type
article
Source
BMC Psychiatry. 23(1)
Subject
Biological Psychology
Biomedical and Clinical Sciences
Clinical Sciences
Psychology
Biomedical Imaging
Neurosciences
Brain Disorders
Clinical Research
Depression
Bioengineering
Serious Mental Illness
Major Depressive Disorder
Mental Health
4.1 Discovery and preclinical testing of markers and technologies
4.2 Evaluation of markers and technologies
Detection
screening and diagnosis
Neurological
Mental health
Humans
Depressive Disorder
Major
Prospective Studies
Reproducibility of Results
Brain
Neuroimaging
Magnetic Resonance Imaging
Artificial Intelligence
Classification
Biomarkers
Deep learning
Harmonization
Predictors
MRI
Public Health and Health Services
Psychiatry
Clinical sciences
Epidemiology
Clinical and health psychology
Language
Abstract
BackgroundEfforts to develop neuroimaging-based biomarkers in major depressive disorder (MDD), at the individual level, have been limited to date. As diagnostic criteria are currently symptom-based, MDD is conceptualized as a disorder rather than a disease with a known etiology; further, neural measures are often confounded by medication status and heterogeneous symptom states.MethodsWe describe a consortium to quantify neuroanatomical and neurofunctional heterogeneity via the dimensions of novel multivariate coordinate system (COORDINATE-MDD). Utilizing imaging harmonization and machine learning methods in a large cohort of medication-free, deeply phenotyped MDD participants, patterns of brain alteration are defined in replicable and neurobiologically-based dimensions and offer the potential to predict treatment response at the individual level. International datasets are being shared from multi-ethnic community populations, first episode and recurrent MDD, which are medication-free, in a current depressive episode with prospective longitudinal treatment outcomes and in remission. Neuroimaging data consist of de-identified, individual, structural MRI and resting-state functional MRI with additional positron emission tomography (PET) data at specific sites. State-of-the-art analytic methods include automated image processing for extraction of anatomical and functional imaging variables, statistical harmonization of imaging variables to account for site and scanner variations, and semi-supervised machine learning methods that identify dominant patterns associated with MDD from neural structure and function in healthy participants.ResultsWe are applying an iterative process by defining the neural dimensions that characterise deeply phenotyped samples and then testing the dimensions in novel samples to assess specificity and reliability. Crucially, we aim to use machine learning methods to identify novel predictors of treatment response based on prospective longitudinal treatment outcome data, and we can externally validate the dimensions in fully independent sites.ConclusionWe describe the consortium, imaging protocols and analytics using preliminary results. Our findings thus far demonstrate how datasets across many sites can be harmonized and constructively pooled to enable execution of this large-scale project.